Device for performing trans-anal minimally invasive surgery having foam support housing

ABSTRACT

An access device for surgical procedures includes an end cap having a rigid body with a flexible support sealingly mounted to the rigid body with at least one separate access port for accommodating introduction of individual surgical instruments into a body of a patient. The at least one access port is sealingly attached to the flexible support and extend in a proximal direction therefrom. The flexible support is of a material more flexible than those of the rigid body and the at least one access port to provide for relative angular movement of the at least one access port to provide flexibility for positioning surgical instruments introduced through the at least one access port.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Continuation of U.S. patent application Ser. No.15/790,582, filed Oct. 23, 2017, the contents of which is incorporatedherein by reference in its entirety.

BACKGROUND OF THE INVENTION 1. Field of the Invention

The subject invention is directed to surgical access devices, and moreparticularly, to multi-port access devices for minimally invasivesurgical procedures.

2. Description of Related Art

Laparoscopic or “minimally invasive” surgical techniques are becomingcommonplace in the performance of procedures such as cholecystectomies,appendectomies, hernia repair and nephrectomies. Benefits of suchprocedures include reduced trauma to the patient, reduced opportunityfor infection, and decreased recovery time. Such procedures commonlyinvolve filling or “insufflating” the abdominal (peritoneal) cavity witha pressurized fluid, such as carbon dioxide, to create what is referredto as a pneumoperitoneum.

The insufflation can be carried out by a surgical access device equippedto deliver insufflation fluid, or by a separate insufflation device,such as an insufflation (veress) needle. CONMED Corporation of Utica,N.Y., USA has developed unique surgical access devices that permit readyaccess to an insufflated surgical cavity without the need forconventional mechanical seals, and it has developed related gas deliverysystems for providing sufficient pressure and flow rates to such accessdevices, as described in whole or in part in U.S. Pat. Nos. 7,854,724and 8,795,223, the disclosures of which are both herein incorporated byreference in their entireties.

During typical laparoscopic procedures, a surgeon makes three to foursmall incisions, usually no larger than about twelve millimeters each.Typically the surgical access device is inserted into an incision usinga separate inserter or obturator placed therein. Following insertion,the inserter is removed, and the trocar allows access for instruments tobe inserted into the abdominal cavity.

A variety of larger access devices are also known in the art foraccessing a surgical site through a single relatively large incision toperform minimally invasive procedures, rather than through multiplesmall incisions. Examples of such devices are disclosed in U.S. PatentApplication Publication No. 2013/0012782, the disclosure of which isherein incorporated by reference in its entirety.

Trans-anal minimally invasive surgery (TAMIS) is a specialized minimallyinvasive approach to removing benign polyps and some cancerous tumorswithin the rectum and lower sigmoid colon. The benefit of TAMIS is thatit is considered an organ-sparing procedure, and is performed entirelythrough the body's natural opening, requiring no skin incisions to gainaccess to a polyp or tumor. This scar-free recovery provides a quickreturn to normal bowel function. Unlike traditional surgery where amajor portion of the large intestine is removed, with TAMIS the surgeonwill precisely remove the diseased tissue, leaving the rest of thenatural bowel lumen intact to function normally. Traditional surgeryoften requires a large incision and a hospital stay ranging from a fewdays to more than a week. A TAMIS procedure may only require anovernight stay in the hospital or can be performed as an outpatientprocedure, often permitting patients an immediate return to an activelifestyle. TATMe (Trans-anal Total Mesorectal Excision) is a moresignificant trans-anal procedure.

It would be beneficial to provide a single incision access device havingmultiple ports with a variety of different port sizes to give a surgeonmore options for instrument introduction during a laparoscopic surgicalprocedure. It would also be beneficial to provide an access devicehaving multiple ports with a variety of different port sizes thatenables ready access to natural orifices for performing trans-analminimally invasive surgical procedures or the like.

SUMMARY OF THE INVENTION

An access device for surgical procedures includes an end cap having arigid body with a flexible support sealingly mounted to the rigid bodywith at least one separate access port for accommodating introduction ofindividual surgical instruments into a body of a patient. The at leastone access port is sealingly attached to the flexible support and extendin a proximal direction therefrom. The flexible support is of a materialmore flexible than those of the rigid body and the at least one accessport to provide for relative angular movement of the at least one accessport to provide flexibility for positioning surgical instrumentsintroduced through the at least one access port.

The flexible support can include a flexible foam material including atleast one of a rubber material, a rubber-like material, a VersaFlexmaterial available from VersaFlex Incorporated of Kansas City, Kans.,and/or a foam material made from a gel or gel-like material. The foammaterial can be a closed-cell foam for providing sealing to prevent gasflow therethrough. It is also contemplated that an open-cell foam withan air tight coating can be used. The access ports can be mounted to adistal surface of the flexible support and extend proximally throughrespective bores in the flexible support to extend proximally from theflexible support. Each access port can include an axially opposed pairof gripping rims with a portion of the flexible support gripped betweenthe gripping rims. The flexible support can have a respective receptaclegroove defined therein for receiving each of the gripping rims.

There can be a plurality of access ports, e.g., three, extendingproximally from the end cap, evenly spaced circumferentially about theend cap. Each access port can extend from a respective planar facet ofthe flexible support. Each access port can extend normal from therespective facet of the flexible support. The respective facets can meetat facet junctures, wherein the facet junctures meet each other at anapex of the flexible support. Each facet can be angled at an angle afrom a circumferential plane of the end cap. The angle a can be largerthan 0° and less than or equal to 60°. All three access ports can be ofa uniform size with one another.

The rigid body can define a complete circumferential ring wherein theflexible support is mounted within and spans the circumferential ringforming a complete circumferential seal between the rigid body and theflexible support. The flexible support can be adhered to an inwardfacing surface of the circumferential ring. The circumferential ring caninclude a proximal ring portion and a distal ring portion, wherein theflexible support is squeezed between the proximal and distal ringportions. The flexible support can define a respective ring groove forreceiving the proximal and distal ring portions.

A bottom body can be included in the access device, having a distallyextending tubular body with an access channel defined therethrough foraccommodating surgical instruments from the access ports into the rectalcavity or natural orifice of a patient. The bottom body can include angas inlet in fluid communication with the access channel. The one ormore access ports can be configured to form a mechanical seal forinsufflation gas for when instruments are inserted through the accessports and when no instruments are inserted through the access ports. Thetubular body can be configured for introduction through a naturalorifice of a body lumen or through a single incision formed in the wallof the abdominal cavity of a patient. The tubular body can be configuredfor trans-anal introduction. The end cap can be configured for complete360° axial rotation relative to the bottom body. The tubular body can bemounted to a main ring portion of the bottom body, and wherein thetubular body is of a less rigid material than that of the main ringportion. The rigid body can include at least one flexible tab configuredto engage and disengage the bottom body to selectively permit or preventrelative axial rotation of the multiport end cap and bottom body. Eachof the access ports can include a respective seal configured to sealagainst gas flow when no surgical instrument is introduced therethrough,and to seal around surgical instruments introduced therethrough.

These and other features of the systems and methods of the subjectdisclosure will become more readily apparent to those skilled in the artfrom the following detailed description of the preferred embodimentstaken in conjunction with the drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

So that those skilled in the art to which the subject disclosureappertains will readily understand how to make and use the devices andmethods of the subject disclosure without undue experimentation,preferred embodiments thereof will be described in detail herein belowwith reference to certain figures, wherein:

FIG. 1 is a perspective view of an exemplary embodiment of an accessdevice constructed in accordance with the present disclosure, showingthe flexible tab and teeth configured to selectively permit or preventrelative axial rotation of the multiport end cap;

FIG. 2 is an exploded perspective view of the access device of FIG. 1,showing the multiport end cap removed from the bottom body;

FIG. 3 is a plan view of the access device of FIG. 1, showing the twoopposed flexible tabs viewed looking distally;

FIG. 4 is a plan view of the access device of FIG. 1, showing the twoopposed flexible tabs viewed looking proximally;

FIG. 5 is a side elevation view of the access device of FIG. 1, showinga connection port for a tube set;

FIG. 6 is a cross-sectional side elevation view of the access device ofFIG. 1, showing the sealing ring of the end cap sealing against theproximal rim of the bottom body;

FIG. 7 is a cross-sectional side elevation view of the access device ofFIG. 1, showing the flexible tabs engaging the teeth of the bottom body;

FIG. 8A is a cross-sectional side elevation view of a portion of theaccess device of FIG. 1, showing a pivoting hinge instead of complianthinge for the flexible tabs;

FIG. 8B is a perspective view of a portion of the access device of FIG.1, showing the end cap;

FIG. 9 is a side elevation view of the end cap of FIG. 8, showing theangle of the facet junctures of the end cap;

FIG. 10 is a plan view of the end cap of FIG. 8, showing the teeth ofthe flexible tabs;

FIG. 11 is a plan view of a portion of the end cap of FIG. 8, showingthe teeth of one of the flexible tabs;

FIG. 12 is a side elevation view of one of the access ports of the endcap of FIG. 8, showing the bellow;

FIG. 13 is a cross-sectional side elevation view of the access port ofFIG. 12, showing the cross-section of the bellow;

FIG. 14 is a side elevation view of another embodiment of an end capconstructed in accordance with the present disclosure, showing bellowswith accordion cross-sections;

FIG. 15 is a cross-sectional side elevation view of the end cap of FIG.14, showing the cross-section of one of the bellows;

FIG. 16 is a perspective view of another exemplary embodiment of an endcap constructed in accordance with the present disclosure, showing twoflexible supports, one including a single bellow and one including adouble bellow;

FIG. 17 is an exploded perspective view of the end cap of FIG. 16,showing rigid bellow supports with support ribs to inhibit inversion ofthe bellows;

FIG. 18 is a perspective view of the double bellow of FIG. 16;

FIG. 19 is a perspective view of another exemplary embodiment of an endcap constructed in accordance with the present disclosure, showing asingle flexible support with three bellows;

FIG. 20 is an exploded perspective view of the end cap of FIG. 19,showing a rigid bellow support with support ribs to inhibit inversion ofthe bellows;

FIG. 21 is a perspective view of the triple bellow of FIG. 19;

FIG. 22 is a perspective view of another exemplary embodiment of an endcap constructed in accordance with the present invention, showing aflexible body that includes a flexible foam material;

FIG. 23 is an exploded perspective view of the end cap of FIG. 22,showing the rigid body separated from the flexible foam support;

FIG. 24 is a perspective view of another exemplary embodiment of an endcap constructed in accordance with the present invention;

FIG. 25 is an exploded perspective view of the end cap of FIG. 24,showing the access ports separated from the flexible foam support;

FIG. 26 is a plan view of the end cap of FIG. 24, showing the flexibletabs;

FIG. 27 is a cross-sectional side elevation view of the end cap of FIG.24, showing the attachment of one of the access ports to the flexiblefoam support;

FIG. 28 is a cross-sectional side elevation view of a portion of the endcap of FIG. 24, showing the gripping rims of one of the access portsgripping the flexible support;

FIG. 29 is an exploded perspective view of one of the access portsconstructed in accordance with an exemplary embodiment, showing the sealguard;

FIG. 30 is a side elevation view of the access port of FIG. 29, showingthe cap mounted on the proximal end of the surgical port body;

FIG. 31 is a cross-sectional side elevation view of a portion of theaccess port of FIG. 29, showing the bases of the main and duck billseals fixed between the cap and the surgical port body with the base ofthe seal guard floating unfixed relative to the cap and surgical portbody;

FIG. 32 is a side elevation view of the seal guard of FIG. 29, showingthe access slits;

FIG. 33 is distal end view of the seal guard of FIG. 32, showing thecircumferential spacing of the access slits; and

FIG. 34 is a schematic view of the access device of FIG. 1, showingaccess ports 40 that vary in size relative to one another.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Reference will now be made to the drawings wherein like referencenumerals identify similar structural features or aspects of the subjectdisclosure. For purposes of explanation and illustration, and notlimitation, a partial view of an exemplary embodiment of an accessdevice in accordance with the disclosure is shown in FIG. 1 and isdesignated generally by reference character 10. Other embodiments ofaccess devices in accordance with the disclosure, or aspects thereof,are provided in FIGS. 2-34, as will be described. The systems andmethods described herein can be used for single incision/natural orificesurgical access, such as for trans-anal minimally invasive surgicalprocedures, with multiple ports. Commonly assigned U.S. PatentApplication Publication Nos. 2016/0287817 and 2017/0056064 areincorporated by reference herein in their entireties. U.S. PatentApplication Publication No. 2017/0050011 is incorporated by referenceherein in its entirety.

The access device 10 for surgical procedures includes a multiport endcap 20 and a bottom body 30. The end cap includes a plurality ofseparate access ports 40 for accommodating introduction of individualsurgical instruments into a body of a patient. The access ports 40extend in a proximal direction, i.e., upwards as oriented in FIG. 1. Thebottom body 30 has a distally extending, i.e. downward extending asoriented in FIG. 1, tubular body 8 with an access channel 9, shown inFIGS. 6-7, defined therethrough for accommodating surgical instrumentsfrom the access ports 40 into the body of a patient. The tubular body 8is mounted to a main ring portion 6 of the bottom body 30. The tubularbody 8 is of a less rigid material than that of the main ring portion 6.The tubular body 8 is configured for introduction into a patient's body,e.g., for trans-anal introduction, or through a single incision formedin the wall of the abdominal cavity of a patient. The bottom body 30includes suture tie downs 22, which are identified in FIG. 4. After thetubular body 8 of bottom body 30 is inserted into a body cavity orincision, the end cap 20 can be attached to the bottom body 30 toprovide gas seal functionality.

The bottom body 30 includes an insufflation gas inlet 14 in fluidcommunication with the access channel 9 through tubular body 8. Theinsufflation gas inlet 14 shown in FIG. 5 is configured to receive atube set with one or more lumens, e.g., a double lumen tube set, howeverthose skilled in the art will readily appreciate that any other suitabletype of inlet can be used without departing from the scope of thisdisclosure. The access ports 40 are configured to form mechanical sealsfor insufflation gas for when instruments are inserted through theaccess ports 40, and when there are no instruments inserted through theaccess ports 40.

With reference now to FIG. 2, the end cap 20 includes a distallyextending seal ring 2. The seal ring 2 of the end cap 20 is receivedinside and seals against a proximal rim 3 of the bottom body 30. The endcap 20 includes a radially protruding stopper rim 5 that abuts aproximal most surface 19 of bottom body 30. An elastomeric seal ring 12forms a seal between the seal ring 2 of the end cap 20 and the proximalrim 3 of the bottom body 30 to provide sealing even during relativerotation of the end cap 20 and bottom body 30 about the longitudinalaxis A. The elastomeric seal 12 is seated in a circumferential channel13 defined in the seal ring 2.

The bottom body 30 includes a plurality of circumferentially spacedapart teeth 18 on the outside of the proximal rim 3. The end cap 20includes an opposed pair of flexible tabs 16, shown in FIGS. 3-4, withdistal teeth 32 thereon that extend radially inward, as shown in FIGS.10 and 11, configured to engage and disengage the radially outwardlyextending teeth 18 of the bottom body 30 to selectively permit orprevent relative axial rotation of the multiport end cap 20 around thelongitudinal axis A.

With reference now to FIGS. 7 and 8A, each of the flexible tabs 16includes a proximally extending manipulation member 17 and a complianthinge member 24 between the manipulation member and the distal teeth 32of the flexible tab 16. In FIG. 7, hinge member 24 is shown as acompliant hinge member, however it can also be a pivoting hinge member24 as shown in FIG. 8A. The flexible tabs 16 are integral with the endcap 20, and are connected to the end cap 20 by the complaint hingemembers 24. Since there are there are two circumferentially opposedflexible tabs 16, squeezing the manipulation members 17 together, i.e.,radially inward towards one another, releases the teeth 32 of theflexible tabs 16 from the teeth 18 of the bottom body 30 to allowrotation of the end cap 20 relative to the bottom body 30 around thelongitudinal axis A. The end cap 20 is configured for complete 360°axial rotation relative to the bottom body 30. Releasing the flexibletabs 16 re-engages the teeth 18 and 32 to prevent further rotation. Thebottom body 30 includes a latching surface 23, labeled in FIG. 8A,proximal to the teeth 18 thereof. The flexible tabs 16 latch with thelatching surface 23 to prevent axial movement of the end cap away fromthe bottom body when the teeth 18 and 32 are engaged, and can even staylatched when the teeth 18 and 32 are disengaged during relative axialrotation of the end cap 20 and the bottom body 30 to prevent axialdisplacement of the end cap 20 relative to the bottom body 30 duringrotation. Optional feedback member 11 cams against the cam 7 to increaseforce feedback as a user squeezes manipulation members 17 to preventover squeezing to keep latching surface 23 engaged to the teeth 32 whenrotating end cap 20 without axially removing it from bottom body 30. Theproximal rim 3 is sandwiched between the seal ring 2 and teeth 32 of endcap 20, as shown in the cross-section of FIG. 7.

With reference now to FIG. 8B, there are three access ports 40 extendingproximally from the end cap 20. As shown in FIGS. 3 and 10, the accessports 40 are evenly spaced circumferentially about the end cap 20, andall three access ports 40 can be of a uniform size with one another, orcan vary in size. Each access port 40 includes a rigid cannula body 42and a cannula cap 44 housing a seal assembly 50, shown in FIG. 6, forsealing against surgical instruments passing through the respectiveaccess port 40. Each cannula body 42 is permanently attached in an airtight manner to a bellow 4, e.g. of an elastomeric material, which is inturn permanently attached in an air tight manner to the respective facet25 of end cap 20, e.g., by adhesive, ultrasound welding, over molding,or any other suitable joining process). The flexibility of bellow 4allows for relative movement of the rigid cannula bodies 42 with respectto one another to provide flexibility and movement for surgical devicesinserted through access ports 40.

Each access port 40 extends from a respective planar facet 25 of the endcap 40. Each access port 40 extends normal from the respective facet 25of the end cap 20. The respective facets 25 meet at facet junctures 27,wherein the facet junctures meet each other at an apex 29 of the end cap20. As shown in FIG. 9, each facet 25 is angled at an angle a from acircumferential plane of the end cap 20, e.g., relative to a planeparallel to rim 5. The angle a is larger than 0° and less than or equalto 60°.

With reference now to FIG. 12, an access port with another embodiment ofa bellow 52 is shown, wherein the base 53 of the bellow 52 is circular.As shown in FIG. 13, bellow 52 forms a flexible support with a singlesigmoidal cross-section that positions a distal end 51 of the at leastone access port 40 within the multiport end cap, represented in FIG. 13by the dashed line, and as shown in the cross sections of FIGS. 6 and 7.The flexible supports, e.g., including bellows 52, described herein caninclude at least one of a rubber material, a rubber-like material,and/or a VersaFlex material available from VersaFlex Incorporated ofKansas City, Kans.

Referring now to FIG. 14, another exemplary embodiment of an accessdevice 100 for surgical procedures includes a multiport end cap 120having a rigid body 102 with flexible supports 154 sealingly mounted tothe rigid body 102 with a plurality of separate access ports 40 foraccommodating introduction of individual surgical instruments into abody of a patient, much as described above with respect to access device10. Each of the access ports 40 is sealingly attached to a respectiveone of the flexible supports 154 and extends in a proximal directiontherefrom, i.e., in an upwards direction as oriented in FIG. 14. Theflexible supports 154 are of a material more flexible than those of therigid body 102 and access ports 40 to provide for relative angularmovement of the access ports 40 to provide flexibility for positioningsurgical instruments introduced through the access ports 40. Each of theflexible supports 154 includes a flexible bellow with an accordioncross-section, as shown in FIG. 15, which spaces a distal end 55 of therespective access port 40 proximally from the multiport end cap 20.

With reference now to FIG. 16, another exemplary embodiment of an endcap 60 is shown. Whereas the bellows 52 and 154 in FIGS. 12-15 have aperimeter shape about the respective access ports that is round, in endcap 60, the bellows 66 have diamond shaped perimeters around therespective access ports 40. As shown in FIG. 17, the rigid body of endcap 60 includes a rigid top body 62 and a two rigid bellow supports 72and 74. The rigid top body 62 and the rigid bellow supports 72 and 74compress an outer peripheral edge 67 of the flexible supports 64 and 65therebetween axially, e.g., by ultrasound welding, adhesive, or anyother suitable joining technique, to form a sealing engagement betweenthe rigid body of the end cap 60 and the flexible supports 64 and 65.The rigid bellow supports 72 and 74 each include a respective supportrib 76 and 78 extending proximally from the rigid bellow support 72 and74 into the respective bellow 66 to inhibit inversion of the bellow 66during instrument insertion into the access port 40.

Each access port 40 can include a compression ring 68 engaged to thedistal end 51 of the access port 40. An inner edge 69 of the flexiblesupports 64 and 65 compressed between the respective access port 40 andthe compression ring 68 to form a sealing engagement between the accessports 40 and the flexible supports 64 and 65. Each paired access port 40and compression ring 68 include an axially opposed pair of respectivegripping rims 71 and 73 with a portion of the respective flexiblesupport 64 and 65 gripped between the gripping rims 71 and 73. Eachflexible support has a respective receptacle groove 75 defined thereinfor engaging each of the gripping rims 71 and 73. Each of the accessports 40 includes a respective seal, much like seal assembly 50described above, configured to seal against gas flow when no surgicalinstrument is introduced therethrough, and to seal around surgicalinstruments introduced therethrough.

As with end cap 20 described above, end cap 60 includes three accessports 40 extending proximally from the end cap 60. One of the accessports 40 connects to the rigid body of end cap 60 through the flexiblesupport 65, wherein the flexible support 65 has a single bellow 66. Theremaining two access ports 40 connect to the rigid body of end cap 60through the flexible support 64, wherein the flexible support 64 has twobellows 66, i.e., a double bellow, as shown in FIG. 18, one for each ofthe two access ports 40.

With reference again to FIG. 17, the rigid bellow support 72 of therigid support includes two respective support ribs 76 extendingproximally from the rigid support 72 into each one of the two bellows66, respectively, to inhibit inversion of the two bellows 66 duringinstrument insertion into the access port 40. The rigid bellow support74 includes a single support rib 76 extending proximally from the rigidsupport 74 into the respective bellow 66 for the same purpose.

Referring now to FIG. 19, another exemplary embodiment of an end cap 80much like end caps 20 and 60 described above is shown with diamondshaped bellows 66. The three access ports 40 connect to the rigid bodyof end cap 80 through the flexible support 84, wherein the flexiblesupport 84 has three bellows 66, i.e., a triple bellow as shown in FIG.21, one for each of the three access ports 40. As shown in FIG. 20, therigid body of end cap 80 includes a rigid top body 82 and a single rigidbellow support 86. The rigid top body 82 and the rigid bellow support 86compress an outer peripheral edge 87 of the flexible support 84therebetween to form a sealing engagement between the rigid body of theend cap 80 and the flexible support 84. Three respective support ribs 88extending proximally from the rigid support 86 into each one of thethree bellows 66, respectively, to inhibit inversion of the bellows 66during instrument insertion into the access ports 40.

With reference now to FIG. 22, another exemplary embodiment of an accessdevice 200 is shown for surgical procedures. Access device 200 includesa multiport end cap 220 having a rigid body 204 with a flexible support206 sealingly mounted to the rigid body 204 with a plurality of separateaccess ports 40 as described above for accommodating introduction ofindividual surgical instruments into a body of a patient.

A bottom body 230 is included in the access device 200, having adistally extending tubular body 202 with an access channel definedtherethrough for accommodating surgical instruments from the accessports 40 into the body of a patient as in embodiments described above.The bottom body 230 includes a connection port 203 for connecting a tubeset with one or more lumens in fluid communication with the accesschannel much as described above with respect to access device 10. Theaccess ports 40 are configured to form mechanical seals for insufflationgas for when instruments are inserted through the access ports 40, andwhen there are no instruments inserted though the access ports 40. Thetubular body 202 is mounted to a main ring portion 207 of the bottombody 230, and wherein the tubular body 202 is of a less rigid materialthan that of the main ring portion 207. The tubular body 202 isconfigured for introduction through a natural orifice of a body lumen orthrough a single incision formed in the wall of the abdominal cavity ofa patient, for trans-anal introduction, or any other suitable mode ofintroduction.

As in embodiments described above, the end cap 220 is configured forcomplete 360° axial rotation relative to the bottom body 230 aboutlongitudinal axis A. The rigid body includes at least one flexible tab216 configured to engage and disengage the bottom body 230 toselectively permit or prevent relative axial rotation of the multiportend cap 220 and bottom body 230 as described above with respect toaccess device 10. Each of the access ports 40 includes a respective sealassembly as described with respect to embodiments above.

The access ports 40 are sealingly attached to the flexible support 206and extend in a proximal direction therefrom, i.e. upwards as orientedin FIG. 22. The flexible support 206 is of a material more flexibleand/or stretchable than those of the rigid body 204 and access ports 40to provide for relative angular movement of the access ports 40 toprovide flexibility for positioning surgical instruments introducedthrough the access ports.

With reference now to FIG. 23, the flexible support 206 includes aflexible, closed-cell foam material for providing sealing to prevent gasflow therethrough; however it is also contemplated that an open-cellfoam material can be used with an air tight coating. It is alsocontemplated that the foam material can include at least one of a rubbermaterial, a rubber-like material, a VersaFlex material available fromVersaFlex Incorporated of Kansas City, Kans., and/or a foam materialmade from a gel or gel-like material. The access ports 40 are mounted toa distal surface of the flexible support 206, i.e. the bottom surface offlexible support 206 as oriented in FIG. 23, and extend proximallythrough respective bores 209 in the flexible support 206 to extendproximally from the flexible support 206. The rigid body 204 defines acomplete circumferential ring wherein the flexible support 206 ismounted within and spans the circumferential ring forming a completecircumferential seal between the rigid body 204 and the flexible support206. The flexible support 206 is adhered, ultrasonic welded, clamped orjoined by any other suitable joining technique to an inward facingsurface 211 of the circumferential ring to form a gas tight seal betweenthe flexible support 206 and the rigid body 204.

As with embodiments described above, there are three access ports 40extending proximally from the end cap 220, evenly spacedcircumferentially about the end cap 220, and uniform in size with oneanother, however it is also contemplated that in an end cap can haveports of sizes that differ from one another as shown schematically inFIG. 34. Each access port 40 extends from a respective planar facet 225of the flexible support 206. Each access port 40 extends normal from therespective facet 225 of the flexible support. The respective facets 225meet at facet junctures 227, wherein the facet junctures 227 meet eachother at an apex 229 of the flexible support 206. Each facet 225 isangled at an angle a from a circumferential plane of the end cap 220.The angle a is not labeled in FIG. 23, but see angle a labeled in FIG. 9as described above. The angle a is larger than 0° and less than or equalto 60°. It is also contemplated that the flexible support 206 can beflat, e.g. where angle a is equal to 0°.

With reference now to FIG. 24, another exemplary embodiment of an accessdevice 300 is shown, including a flexible support 306 as described abovewith respect to access device 200. As shown in FIG. 25, thecircumferential ring of rigid body 304 includes a proximal ring portion313 and a distal ring portion 314. As shown in FIGS. 26-27, the flexiblesupport 306 is squeezed between the proximal and distal ring portions313 and 314. The flexible support 306 defines a respective ring groove315 (labeled in FIGS. 25 and 28) in its proximal and distal surfaces forreceiving circumferential rims of the proximal and distal ring portions313 and 314. The proximal and distal portions 313 and 314 can besealingly joined to the flexible support 306 by ultrasonic welding,adhesive, or any other suitable joining technique.

Each access port 40 includes an axially opposed pair of gripping rims321, including a proximally extending gripping rim 321 defined on acompression ring 323 joined to the distal end of each access port 40. Aportion of the flexible support 306 is gripped between the respectivegripping rims 321 of each access port 40. The flexible support 306 has arespective receptacle groove 325 defined therein for receiving each ofthe gripping rims 321.

With reference now to FIG. 29, at least one of the access ports 40 caninclude a surgical port assembly that provides mechanical sealing forsurgical instruments to reduce loss of pressure during surgicalprocedures. The assembly includes a tubular surgical port body 402extending from an upper surface of the end cap, e.g., any of the endcaps described above, and defining an access channel 401 therethrough. Acap 404 is mounted to a proximal end of the surgical port body 402 andopens into the access channel 401 of the surgical port body 402, asshown in FIGS. 30 and 31. A main seal 406 has a base 407 that is fixedbetween the cap 404 and the surgical port body 402 to suspend the mainseal 406 across the access channel 401 as shown in FIG. 31 to providemechanical sealing against surgical instruments extending through theaccess channel 401. A duck bill seal 408 is included distal from themain seal 406 within the access channel 401. The duck bill seal 408includes a base 409 that is fixed between the cap 404 and the surgicalport body 402 and provides mechanical sealing against surgicalinstruments extending through the access channel 401 in addition to thesealing provided by main seal 406.

A seal guard 412 is seated in an unfixed manner between the cap 404 andthe main seal 406 within the access channel 401. The seal guard 412 isof a material that is more rigid that those of the main seal 406 and theduck bill seal 408 to provide protection for the main seal 406 and theduck bill seal 408 when instruments are inserted through access channel401, and to prevent inversion of the main seal 406 and/or the duck billseal 408, e.g., when surgical instruments are withdrawn from accesschannel 401.

With continued reference to FIG. 31, the seal guard 412 extends acrossthe access channel 401 and is configured to move relative to the cap 404and the surgical port body 402 to accommodate movement of surgicalinstruments extending through the access channel 401. The seal guard 412can move relative to the bases 407 and 407 of the main seal 406 and duckbill seal 408. This movement is accommodated by the seating of the base413 of the seal guard 412 about the inward rim 403 of cap 404 withinaccess channel 401. Since it is free to move relative to the cap 404 andthe surgical port body 402, the seal guard 412 can accommodate movementof instruments relative to surgical port body 402 and therefore improvesealing against the instruments by the main seal 406 and duckbill seal408 relative to the sealing that would be accomplished if the seal guard412 was rigidly mounted relative to the cap 404 and the surgical portbody 402.

As shown in FIGS. 32 and 33, the seal guard 412 defines eight evenlyspaced access slits 414 therethrough in a distal, frustoconical sectionof the seal guard 412. The access slits are spaced circumferentiallyabout the central aperture 215 of the seal guard 412 for passage ofsurgical instruments through the seal guard 412, accommodated by thedeflectable panels separated by the access slits 414. The access slits414 facilitate alignment of surgical instruments with openings throughthe main seal 406 and the duck bill seal 408 to reduce leakage ofpressurized gas through the main seal 406 and duck bill seal 408 duringsurgery.

The methods and systems of the present disclosure, as described aboveand shown in the drawings, provide for single incision/natural orificesurgical access with superior properties including minimally invasive,multiple port access with flexibility for relative movement of theaccess ports. While the apparatus and methods of the subject disclosurehave been shown and described with reference to preferred embodiments,those skilled in the art will readily appreciate that changes and/ormodifications may be made thereto without departing from the scope ofthe subject disclosure.

1. An access device for surgical procedures comprising: an end capincluding a rigid body with a flexible support sealingly mounted to therigid body with at least one separate access port for accommodatingintroduction of individual surgical instruments into a body of apatient, the at least one access port sealingly attached to the flexiblesupport and extending in a proximal direction therefrom, wherein theflexible support is of a material more flexible than those of the rigidbody and the at least one access port to provide for relative angularmovement of the at least one access port to provide flexibility forpositioning surgical instruments introduced through the at least oneaccess port, wherein the flexible support includes a flexible foammaterial including at least one of a rubber material, a rubber-likematerial, a VersaFlex material, and/or a foam material made from a gelor gel-like material.
 2. (canceled)
 3. The access device as recited inclaim 1, wherein the foam material is at least one of a closed-cell foamand/or an open-cell foam with an air tight coating for providing sealingto prevent gas flow therethrough.
 4. The access device as recited inclaim 1, wherein the access ports are mounted to a distal surface of theflexible support and extend proximally through respective bores in theflexible support to extend proximally from the flexible support.
 5. Theaccess device as recited in claim 1, wherein each access port includesan axially opposed pair of gripping rims with a portion of the flexiblesupport gripped between the gripping rims.
 6. The access device asrecited in claim 5, wherein the flexible support has a respectivereceptacle groove defined therein for receiving each of the grippingrims.
 7. The access device as recited in claim 1, wherein there are aplurality of access ports extending proximally from the end cap, evenlyspaced circumferentially about the end cap.
 8. The access device asrecited in claim 7, wherein each access port extends from a respectiveplanar facet of the flexible support.
 9. The access device as recited inclaim 8, wherein each access port extends normal from the respectivefacet of the flexible support.
 10. The access device as recited in claim8, wherein the respective facets meet at facet junctures, wherein thefacet junctures meet each other at an apex of the flexible support. 11.The access device as recited in claim 10, wherein each facet is angledat an angle a from a circumferential plane of the end cap.
 12. Theaccess device as recited in claim 11, wherein the angle a is larger than0° and less than or equal to 60°.
 13. The access device as recited inclaim 1, wherein the rigid body defines a complete circumferential ringand wherein the flexible support is mounted within and spans thecircumferential ring forming a complete circumferential seal between therigid body and the flexible support.
 14. The access device as recited inclaim 13, wherein the flexible support is adhered to an inward facingsurface of the circumferential ring.
 15. The access device as recited inclaim 13, wherein the circumferential ring includes a proximal ringportion and a distal ring portion, wherein the flexible support issqueezed between the proximal and distal ring portions.
 16. The accessdevice as recited in claim 15, wherein the flexible support defines arespective ring groove for receiving the proximal and distal ringportions.
 17. The access device as recited in claim 1, furthercomprising: a bottom body having a distally extending tubular body withan access channel defined therethrough for accommodating surgicalinstruments from the access ports into a rectal cavity, or naturalorifice of a patient.
 18. The access device as recited in claim 17,wherein the bottom body includes a gas inlet in fluid communication withthe access channel.
 19. The access device as recited in claim 18,wherein the one or more access ports are configured to form a mechanicalseal for insufflation gas for when instruments are inserted through theaccess ports and when no instruments are inserted through the accessports.
 20. The access device as recited in claim 17, wherein the tubularbody is configured for trans-anal introduction.
 21. The access device asrecited in claim 17, wherein the end cap is configured for complete 360°axial rotation relative to the bottom body.
 22. The access device asrecited in claim 17, wherein the tubular body is mounted to a main ringportion of the bottom body, and wherein the tubular body is of a lessrigid material than that of the main ring portion.
 23. The access deviceas recited in claim 17, wherein the rigid body includes at least oneflexible tab configured to engage and disengage the bottom body toselectively permit or prevent relative axial rotation of the multiportend cap and bottom body.
 24. The access device as recited in claim 1,wherein each of the access ports includes a respective seal configuredto seal against gas flow when no surgical instrument is introducedtherethrough, and to seal around surgical instruments introducedtherethrough.